Taiwan FDA registration af3f2dd076bbf5e894cb84196ea19fb7

"Combi" McLean full suture suspension device system

TW: “康美”麥克林全縫線懸吊裝置系統

Taiwan·Risk Class 2·Linvatec Corporation d/b/a ConMed Linvatec;; CONMED CORPORATION·Registered Nov 25, 2020 – Nov 25, 2025Expired

Registration details

Analysis ID: af3f2dd076bbf5e894cb84196ea19fb7
Customs Code: DHA05603411304

Company information

Manufacturer: Linvatec Corporation d/b/a ConMed Linvatec;; CONMED CORPORATION
Manufacturer Country: United States
Authorized Representative: WEECON CO., LTD.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N.3030 Single or multiple metallic bone fixation devices and accessories
Import Information: import

Dates and status

Registration Date: Nov 25, 2020
Expiry Date: Nov 25, 2025

About this record

Access comprehensive regulatory information for "Combi" McLean full suture suspension device system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number af3f2dd076bbf5e894cb84196ea19fb7 and manufactured by Linvatec Corporation d/b/a ConMed Linvatec;; CONMED CORPORATION. The authorized representative in Taiwan is WEECON CO., LTD..

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